UK experts discuss the catastrophic failures and criminal conduct of Britain’s Medicines and Health Regulatory Agency (MHRA) in the emergency use authorization of Pfizer/BioNTech COVID-19 injections and boosters. Shockingly, 84% of the entire budget for Britain’s medicines regulatory agency comes from Big Pharma, and the agency’s proper regulatory authority to insure public safety has been gutted by these financial conflicts, and by the separate and parallel regulatory agency under direction of the Bill Gates Foundation, WEF and WHO.
Mr. Andrew Bridgen, Member of Parliament for North West Leicestershire, has been single-handedly exposing the malfeasance of the UK government officials, public health experts and MHRA in failing to protect the public from further disability, damage and deaths with the new data showing the irreparable harm and preventable deaths from the COVID shots. He has also called out British Prime Minister Rishi Sunak for massive financial conflicts of interest related to the approval of a 10-year year business agreement between the UK government and Moderna for “vaccine research,” even worse after the Basel (Switzerland) Cardiovascular Research Institute published the latest peer-reviewed scientific evidence of a 1 in 35 risk of myocarditis after 3 shots of the Moderna mRNA-1273 COVID-19 injection.
In spite of Andrew Bridgen’s courageous efforts based on the actual data to warn government officials and the public of the dangers of the deadly COVID injections, he has been ostracized, called a “conspiracy theorist, and even expelled by his own Party. Mr. Bridgen said his expulsion “confirms the culture of corruption, collusion and cover-ups”. Yet, he continues his dedication to the truth, and to warning the people of Britain and the world of these “toxic by design” COVID injections.
For more information, read here: Andrew Bridgen: MP expelled by Tories after Covid vaccine comments and see his letter to the Prime Minister:
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Co-Host: Hedley Rees, based in the United Kingdom. Mr. Rees has been providing consultancy on the development, manufacture and distribution of drugs that are fully compliant with the GMP requirements of 21 CFR Title 21, since 2005 through his company, PharmaFlow. Prior to that, he spent 16 years in senior roles in Big Pharma (Bayer) and 10 years in biotech (British Biotech, Vernalis and OSI Pharmaceuticals (now Astellas). Mr. Rees also authored Supply Chain Management in the Drug Industry: Delivering Patient Value for Pharmaceuticals and Biologicsfor Wiley, NJ in 2011. His expertise is in the area of anything to do with manufacture through the three phases of clinical trials (and preclinical if required) and ongoing distribution of the commercial supply. Where regulations have been breached, he has a duty to bring this to the attention of regulators, as has been happening with the frozen vials of COVID shots that were shipped only part way finished.
Hedley joins Truth for Health Foundation Team: https://open.substack.com/pub/hedleyrees/p/hedley-joins-truth-for-health-foundation?r=xoehy&utm_campaign=post&utm_medium=web
Follow Hedley Rees on his Substack column, INSIDE PHARMA, where he shares all he can to expose the lies and deceptions that are costing lives and jeopardizing public safety. Watch one of his many interviews here: https://rumble.com/v14gou4-drug-development-expert-sounds-alarm-over-rushed-to-market-covid-19-vaccine.html
Read more on Facts about SARS-CoV-2 Injections (aka DNA vaccines) and advanced therapy medicinal products (ATMPs): https://open.substack.com/pub/hedleyrees/p/facts-about-sars-cov-2-injections?r=xoehy&utm_campaign=post&utm_medium=web Watch Recent interview discussing the violations of manufacturing processes and regulations that are supposed to keep us safe: https://rumble.com/v1qe9nk-freeman-interviews-hedley.html